CA1286944C - Method and means for dispensing respirating gases by effecting a known displacement - Google Patents

Abstract

ABSTRACT OF THE DISCLOSURE
A device for administering oxygen or other respirating gases to a patient premeters and temporarily stores single dose quantities of respirating gas and dispenses each dose in synchronization with the patient's inspiratory cycle. A sensor produces a signal upon the onset of each inhalation and those signals cause single doses of gas to be dispensed to the patient in unison with the patient's respiration cycle.

Description

12~694'~ 1 I~ETHOD AND MEANS FOR DISPENSING
RESPIRATING GASES BY EFFECTING A
~NOWN DISPEACE~ENT
CROSS-REFEP~NCE TO RELATED APPEICATIONS

BACKGROUND OF THE INVENTION
This invention relates generally to methods and apparatus for administering oxygen and other respirating gases to a patient.
More particularly, this invention relates to ~ethods and means for administering oxygen or other gases to a patient on an intermittent, respiration controlled, basis.
It has beco~e common medical practice to treat patients suffering from advanced stages of chronic obstructive pulmonary diseases by administration of oxygen. Such pulmonary diseases, lncluding chronic bronchitis, emphysema and severe asthma, are one of the fastest rising causes of death in the United States affecting probably more than ten million people. It is estimated that more than 500,000 people in the United States either are routinely receiving oxygen therapy or could beneflt from it. Much of thls rather expenslve treatment is funded by Medicare.
The devlces which commonly have been used to deliver oxygen to a patient meter the oxygeD flow at a fixed rate and deliver a constant stream of oxygen to the patient. Oxygen is received by the patlent either through a mask which is placed over the nose and ~outh or through a cannula which terminates in nares inserted into the .
patient's nostrils.
I~ has long ~ been recognized that providing a constant 1Ow of oxyge~ to a patient results in the waste of a substantial proportion of the oxygen supply. The~ normal breathing cycle consists of an inhalatlon, an exhalation longer in duration than the inhaLation, and then a pause before the ne~t cycle. Oxygen supplied to a patient during the exhalatlon~ and pause phases of the resplratory cycle is totally wasted. Devices have~ been developed to conserve oxygen by regulating the oxygen flow, turning it o~ and off, in response to the respiratory cycle~ Typical of such devices are those of Myers, U.S.
~a~ent No. 4,054,133, and Mon, U.S. Patent No. 4,381,002. Each of these paFents disclose devices whlch sense inhalation and exhalat1On ,._ .
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pressures in the nasal cavity of a patient and converts those sensed pressure differentials to signals which control the flow of oxygen to a patient. Typically, oxygen flow is started upon the sensing of a negative pressure relative to atmospheric indicating the start of an 5 inspiration period. Oxygen flow is then stopped at a second signal produced by the sensing of a positive pressure relative to atmospheric indicating the start of the expiration period.
More recently , Dr. Gerald Durkan clinically observed that only the oxygen supplied during the initial part of an inspiration perfod 10 was efficiently absorbed by a patient. It is that first $nspired portion of oxygen which reaches the alveoli while oxygen supplied during the latter part of an inspiration period remains in non-absorbing areas such as the pharynx, trachea and bronchial tubes.
Durkin concluded that supplying oxygen at a high rate, beginning at 15 the start of inspiration but lasting only for a small portion of the inspiration period offered economic and physiologic advantages over those prior techniques which supplied oxygen during the entire inspiration period.
As a result of his observations, Durkan developed a respirator system known as the Demand Oxygen Controller which is disclosed in U.S. Patent No. 4,457,303. That respirator system uses a fluidic laminar proportional amplifier to sense the start of an inspiration period. Oxygen flow to a patient is immediately started in response to the sensed inspiration. Timlng means, also started in response to 25 the sensed insplration, stop the oxygen flow after a preset period of time which is shorter than is the inspiration period. As a result, oxygen is supplied to a patient only during the effective, early stages of an inspiration resulting in an oxygen savings of as much as 70% as compared to a continuous flow administration.
All of these prior art techniques have one property in common.
All determine or control the volume of oxygen (or other respirating gas) delivered to the patient over a respiratory cycle by controlling both the rate at which o~ygen is allowed to flow and the time or duration of oxygen flow Eor each respiratory cycle. Both Myers and 35 Mon teach the starting of oxygen flow upon sensing the beginning of an inspiration and the stopping of oxygen flow upon the sensing of an expiration. Durkin teaches the starting of oxygen flow upon sensing the beginning of an inspiration and stops oxygen flow at the end of a .~ .... , . ,, : . :
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time period which is independent from, and shorter than, the inspiration period.
Those prior art devlces which connect a rate metered supply of oxygen to a cannula for a predetermined time to effect the desired dose delivery all have the disadvantage that both the rate and duration oF flow must ba precisely contro~led if the dose is to be accurately measured and dispensed. Because of the small quantities of oxygen required per dose (typically about 33cc measured at standard temperature and pressure), it is difficult and expensive on a 10 production basis to provide for the degree of accuracy of flow rate and of timing required to ensure a safe dose effLciently dellvered ~or each breath. An improved and simpli~ied way to dispense an oxygen dose in synchronization with a patient's respiratory cycle provides clear advantages in this art.
SUMMARY OF THE INVENTION
A method and apparatus for administering oxygen or other medical gases to a patient in sychroniæation with the respiratory cycle of the patient operates by generating a signal ln response to the onset of an inhalation and immediately dispenses a premeasured volume of the oxygen or other gas by effecting a known displacement. Displacing means suitable for use include a cylinder con~aining a spring loaded piston which is filled from a pressurized gas supply forcing the piston back to a stop set to control the volume. Other displacing means include a pressurized, ad~ustable volume which is blown down 25 into the cannula for dose delivery.
Hence, it is an ob~ect of this invention to provide a method and means to supply measured doses of respiratlng gases to a patient during the early stages of an inspiration and dispensing a premeasured gas volume by effecting a known displacement.
It is another ob~ect of this invention to provide a simplified respirator apparatus which does not employ timing means to control dose volume.
Other ob~ects of this invention will be apparent from the following description of certaln embodiments of the invention.
; 35 DESC~IPTION OF THE DRAWIN~
Specific embodiments of the invention are illustrated in the ~, drawing in which:
Figure 1 is a schem~tic diagram showing generally the gas supply . .

apparatus of this inventlon;
Figure 2 illustrates ln partial sectio~ one embodiment of a displacement dispenser for use with the gas supply apparatus;
Figure 3 illustrates a rolling diaphragm type of piston 5 displacing means pre~erred in certain embodiments of this invention, Figure 4 is a diagram in partial section of a fixed volume, but adjustable, gas dispensing means;
Figure 5 schematically depicts one specific control circuit preferred -for use with certain embodiments of this invention;
Figure 6 illustrates another control circuit suitable for other embodiments of this invention;
Figure 6 A shows another control circult especially useful with the embodiments of Figures 2 and 4;
Figure 7 depicts an alternative embodiment of this invention 5 including means to prevent over-oxygenation in the event of hyperventilation; and Flgure 8 schematically depicts another control circuit embodiment useful with the dispensing means of this invention.
DESCRIPTION AND DISCUSSIO~ OF THE INVENTION
Various embodiments of this invention will be described and discussed in detail with reference to the drawing figures in whlch like reference numerals refer to the same component or part illustrated in different figures.
Referring first to Figure 19 there is shown in its simplist 25 schematic form the gas supply apparatus of this invention. The device comprises a three-way valve means 20 having its eommon port 20a connected to a displacer or containment means 21 by way of a conduit 22. One of the two option ports 20b is connected by line 23 to a : supply of respirating gas, typically oxygen, 24. Gas delivered 3 through line 23 is maintained at a relatively constant pressure, typi~ally about 20 psig, by means of pressure regulator 25. The other option port, 20c, is connected to a cannula or other delivery system 26 which terminates in nares or mask 27.
In use, with valve 20 in the position shown, oxygen from source 35 24 at the pressure controlled by regulator 25 flows directly to displacer 21. There it effects a pre-set displacement equal to a unit dose, for one breath, of oxygen measured at standard conditions.
Displacer 21 thus performs two distinct functions. First, it :. . :' : .: .. ' , ., , ~ .::
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premeters or measures a quantlty or mass of gas equal to the prescrlbed unit dose for one breath. Second, it temporarlly parks or stores that premetered quantity, or unit dose and then releases that stored ~1nit dose in synchronization with the onset or start of the 5 patient's inhalation. By first premetering and then temporarily storing each single or unit dose of gas, the source of respirating gas is always isolated from direct communication with the patient by the displacer which provldes significant safety features not attalnable with conventional devices.
Displacer 21 may be of two distinct types, each ~ype operating in a different mode but accomplishing essentially the same result. In one type of displacer, gas is mechanically pushed, or displaced frorn, a known volume through action of a piston or similar means. In a second type of displacer which is advantageous to use at high source 5 pressures, there is provided a fixed volume reservoir which is filled or loaded at source pressure and which discharges a unit dose to the patient by releasing, or blowing down, the pressurized gas within the reservoir to essentially atmospheric pressure.
It is conventional to express a unit dose of respirating gas in terms of a gas volume at normal temperature and pressure. Gas dispensing means of this general type typically operate at ordinary room temperature so gas volume changes due to temperature variations may be safely ignored. Hence, the operating volume of both types of displacer or containment means 21 is dependent upon the pressure of the gag source. For example, if the volume of oxygen prescribed for one breath or unit dose is 33cc (approximately equal to a continuous rate of 2 liters per minute), then the required displacement volume the first described type of displacer at a source pressure of 20psig would be about 14cc. Were the second type of described displacer (the embodiment of Figure 4~ to be used, then at a source pressure of 20psig, the reservoir volume required would be about 24cc. In either type of displacer, a change in the prescribed unit dose of respirating gas is accommodated by changing the displaced volume (or blowdown volume) in ways which will later be described. It is, of course, also possible to control, or change, the unit dose by changing the source pressure but that dose size control method is less preferred.
Each dose of oxygen must be delivered in synchronization with the patient's inspiratory cycle. ~o accomplish that synchronous delivery - : - . . :- , - ..................... .

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:,: - : ' , ~ :- . , - ', . -.' ' ' -. ' necessarlly requires an extremely sensltive and fast responding sensor 28 which is operably connected to cannula 26 by means of line 29 so that, for example, it may monitor and respond to slight changes of pressure occurring in the nasal cavity o~ the patient. Exemplary 5 sensors meeting those requirements and known in the prior art include a spring-loaded diaphragm sensor as shown by Myers in U.S. Patent No.
4,054,133 and fluidic devices employing laminar proportional amplifiers as shown by Mon in U.S. Patent No. 4,381,002 and Durkin iQ
U.S. Patent No. 4,457,303. A thermistor-type sensor responsive to lO directional gas flow may also find use in the devices of this invention. Also, a sensitive pressure-to-electric switch, such as the Microswitch, Series 160, may be employed.
Sensor 28 is arranged to produce a signal upon detection of the beginning of an inhalation by the patient. The signal, which may be l~ electrical or pneumatic, is transmitted via means 30 to control circuit 31. Control circuit 31, responding to the signal from sensor 28, activates triggering means 32 causing valve 20 to move to its other position connecting port 20a with port 20c. In this position, oxygen source 24 is isolated from the remainder of the system and the unit dose of oxygen in displacer 21 surges through line 22 and valve into cannula 26 and thence to the patient. A signal 33 is produced by displacer 21 upon completion of the delivery of a unit dose of oxygen causing control circuit 31 to reset valve 20 to its original position thus beginning the cycle anew.

2~ Figure 2 illustrates the gas supply apparatus of Figure 1 which utilizes a piston-type displacer 21. In thi~ embodiment, displacer 21 comprises a piston 40 operating within a cylinder 41. When valve 20 is in the position lllustrated, with port 20a connected to port 20b, oxygen from source 24 enters the end of cylinder 41 through line 22 30 forcing piston 40 back against spring 42 until the end 43 of piston rod 44 engages stop 45. Stop 45, in a preferred embodiment, is ad~ustable so as to allow varying the volume 46 (and hence the unit dose of oxygen administered per breath) withln cylinder 41 when the piston 40 is at the limit of its travel.
: 35 so long as valve 20 is in the position shown, pressure exerted upon the head o~ piston 40 by the gas from source 24 maintains spring 42 under compression and the piston rod end 43 firmly against stop 45.
Upon detection of the start of an inhalation by the patient, sensor 28 ,........... .. . . .. .

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t~ansmits a signal via 30 to control circtltt 31 which in turn callses valve 20 to move to its other position with valve port 20a connected to port 20c. Spring 42 then forces the piston ~0 forward to the end of cylinder ~1 causing the gas within the cylinder to surge through line 22 and valve 20 into cannula 26 and thence to the patient.
sensor 47, which may comprlse a differential pressure switch, a magnetic reed switch or a microswil:ch, is operably arranged through means 48 to detect the completion of the piston travel and to transmit a signal 33 to control circuit 31. Thereupon, valve 20 resets to its lO refill position and the fixed volume 46 i5 refilled ~or ~he next cycle.
One particularly preferred piston and cylinder arrangement for use as the displacer 21 of this invention is ill~lstrated in Figure 3.
This device is commercially available under the tradename Bellofram 15 Rolling Diaphram and is described in detail in U.S. Patent Nos.

3,137,215 and 3,373,236. As shown in Figure 3, the device includes a diaphragm 49 which is for~ed in the shape of a truncated cone with its center fastened to the head of piston 40 and its outer flange clamped to cylinder 41. Diaphragm 49~ alternately rolls and unrolls on the skirt of piston ~lO and the wall of cylinder 41 as the piston travels back and ~orth. The rolling actlon of diaphragm 49 eliminates sliding contact and breakaway friction. The diaphragm arrangement forms a complete seal preventing blow by leakage and pressure loss and requires no lubrication of any kind. These features make the device 25 highly advantageous to use in the dispensing of respirating gases to a patient.
Figure 4 illustrates another embodiment of this invention which is especially useful with higher pressure oxygen sources such as those central systems having distribution lines to multiple locations as in 3 many hospitals and other health care facilities. Those central s-ystems typically maintain an oxygen pressure of about 50 psig in the distribution lines. This embodiment employs a two-position valve 50 having four ports 50a, 50b, 50c and 50d. In the valve position shown9 the gas source 24 is connected through valve ports 50a and 50b and : - 35 line 22 directly ~o a fixed volume chamber 60 within displacer 210 The displacer unit or containment means in this a~bodiment may comprise a piston with a rolIing diaphragm as is illustrated in Figure 3. Unlike the embodiment of Figure 2, however, piston ~1 within .. . ..
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cylinder 62 remains stationary durlng operation of the gas supply apparatus. Provision is made for changing, or set~ing, the volume 60 (in order to ~ix a unit dose of oxygen dispensed per breath) by moving piston 61 up and down through connecting rod 63 which is adapted to lock into ad~ustment rack 64 at the desired volume or unit dose position.
While valve 50 is Ln the first, or fill, posltion sensor 28 is connected via line 29 and valve ports 50c and 50d to the cannula 26.
Upon the detection of the start of an inhalation, sensor 28 produces a signal which is transmitted to control circuit 31 by means 30. That signal may be either pneumatic or electrical depending upon the type of device e~ployed as the sensor 28. The signal from sensor 28 causes control circuit 31 to actuate valve 50 through means 32 and so change the valve to its other position. In this o~her position, valve port 15 50b is connected to port 50d while ports 50a and 50c are isolated from the system. Pressurized gas in fixed volume chamber 60 thus has an open flow path via line 22, through valve 50 to cannula 26 and thence to the patient causing the pressure within chamber 60 to drop rapidly to essentially atmospheric. A differential pressure switch, or other suitable sensor, 65 is connected to chamber 60 through conduit 66 and transmits a signal via means 33 to the control circuit 31 upon depletion of the pressure within chamber 60. This signal causes the control circuit 31 to reset valve 50 back to its original, or refill, position thus ~tarting a new cycle The valving arrangement depicted in this embodiment isolates sensor 28 from the pressure surge which occurs as oxygen flows from chamber 60 to the patient. This arrangement is advantageous in those cases wherein tbe construction of sensor 28 might be damaged by sudden positive over pressures. This valving arrangement may, of course, also be used in the embodiment depic~ed in Figure 2. In addition to simplicity, the compact size of the device of this embodiment may be appreciated by calculation of the volume 60 required to deliver a unit dose of 33cc of oxygen measured at standard conditions. At a system pressure of 50 psig, volume 60 would be set at approximately 10cc to 3~ deliver 33cc of oxygen measured at atmospheric pressure.
Control circuit 31 has been described in functional terms in ; relation ~o the embodiments shown in Figures 1, 2 and 4. Figure 5 illustrates details of a control circuit especially adapted to the ' ~

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embodiment o~ Figure ~ but al80 appropriate for use with t~e embodiment of Figure 2. There is shown a ~our-way, two position valve in the refill position wherein lLne 23 communicates with a source of respirating gas via port 70a and line 22 leads to a displacer via 5 port 70b. Cannula 26 is connected to line 29 and sensor 28 through ports 70c and 70d. Sensor 28 may be of any type having adequate sensittvity to detect the onset of Lnhalation. It may, for example, be a very sensitive pressure switch, a ~luidic amplifier or a thermistor which reacts to flow. Sensor 28, upon detection of the lO onset of an inhalation, produces a trigger signal 72 which activates interval timer 73. Interval timer 73 is of the type commonly called a one-shot timer or a time delay relay which, upon receiving the trigger signal, initiates a timed cycle oE power from power supply 74. This cycle of power, traveling through conductors 75, 76 and 77, activates l~ the solenoid coil 78 of valve 70 causing it to move to its other position wherein port 70b is connected to port 70d and wherein ports 70a and 70c are isolated from the system. At the end of the cycle period, the electric power pulse stops, valve 70 returns to its original, or reset, position~ and the interval timer 73 resets to an "off" position until the next trigger signal. The exact duration of the electric power pulse produced by interval timer 73 is not important 90 long as it is long enough to permit complete delivery of the stored pulse volume in the displacer chamber and short enough to allow sufficient time for the metering chamber (volume 60 of Figure 4) to refill in time for the next cycle. A range of times rom about 3/8 to 3/4 of a second is ~enerally appropriate with a period of 1/2 second being a good design target. It is important to note that dose volume is, within wide limits, completely independent of electric pulse duration; the volume of a unit dose be~ng directly determined by effecting a known displacement.
The control circuit of Yigure 5 may also be modified to employ pneumatic means, rather than the illustrated solenoid coil 78, to cause valve 70 to move from one position to the other. ~n this embodiment, gas stored under pressure in displacer 21 may be used as 35 the motive fluid to power the valve actuator. Gas used to power valve movement need not be wasted but may be discharged into cannula 26 for use by the patient.
~igure 6 illustrates another control circuit which is :: , . . . : . :
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particularly adapted for use with the eMbodlment of Figure 2. The circuit includes a Elip-flop relay ôO in series connection via conductor 81 with a power supply 82, second conductor 83, valve solenoid coil 84 and third conductor 85. Sensor 28, in this 5 embodiment, detects the onset of both an inhalation and an exhalation and transmits a trigger signal to relay 80 upon the occurrence of each event. As shown in the Figure, valve 20 is in the refill position wherein the displacer is in direct communication with a source of respirating gas. Upon receiving a slgnal representative of the onset lO of an inhalation from sensor 28, flip-Elop relay 80 will, through activation of solenoid coil 84, cause valve 20 to move to its other position. The valve 20 in its other position puts the displacer via line 22 into direct communication with cannula 26. Valve 20 remains in this other position until relay 80 receives from sensor 28 a second 15 signal representative of the onset of an exhalation. At that time, relay 80 causes valve 20 to return to its original, or refill, position~ The onset of an inhalation produces a small negative pressure relative to ambient while the onset of an exhalation produces a slight positive pressure relative to ambient. Thus, sensor 28 can 20 be arranged to produce signals of different polarity, corresponding to negative and positive pressures, which ensures that flip-flop relay 80 wlll cause valve 20 to remain in proper synchronization with the breathing cycle of the patient.
Figure 6-A shows yet another variation of control circuit 31 25 which is adaptable for use with the embodiments of both Figures 2 and 4. This embodiment uses a flip-fIop relay 80, as does the circuit of Figure 6, but sensor 28 is arranged to produce a signal only upon the onset of~an inhalation. Upon receiving a signal from sensor 28, relay activates the solenoid coil 84 of the valve means to that valve 30 position wherein a unit dose of oxygen or other respirating gas is delivered from the displacer to the cannula. A signal 33 is received by relay 80 from the displacer (as was described in relation to Figures 2 and 4) when the piston has reached the limit of its travel tFigure 2) or when the pressure within the fixed volume chamber has 3~ depleted to atmospheric (Figure 4). Signal 33 causes relay 80 (and coil 84) to flip to its other, or refill, position thus completing a cycle.

';' ' Flgure 7 depicts another embodiment of the gas supply apparatus of this invention which includes provision for preventing over-oxygenation in the event that ~here ls hyperventilation by the patient. This embodiment employs a two-position valve 90 having four 5 ports 90a, 90b, 90c and 90d. In the valve position illustrated, gas flows from a source (not shown) by way of line 23 through valve ports 90a and 90b and line 22 to the interior of displacement means 95.
Containment means 95 may conveniently be a pis~on 96 with a rolling diaphram 97 disposed within a cylinder as is illustrated in Figure 3.
10 The piston may be arranged to recLprocate back and forth as in the embodiment of Figure 2 or may remain stationary during operation as in the embodiment of Figure 4. In that embodiment employing reciprocation of piston 96~ the resilient restoring ~eans may be provided by a pneumatic chamber 98 rather than the mechanical spring 15 means shown in Figure 2. The magnitude of the pneumatic restoring force may be set at any desired level through adjustment of the gas pressure within chamber 98 by adding gas to or withdrawing gas from chamber 98 by way of valve means 99.
There is also provided a flow rate limiting means 100 located in 20 the gas supply line to the disp~acement means 95. ~n this embodiment, means 100 is preferably located in line 22 between ~alve 90 and displacement means 95 while in the embodlments of Figures 2 and ~, means 100 is preferably located in line 23 upstream of the valve means. Flow rate limiting means 100 may conveniently comprise an orifice sized so that the maximum flow rate of oxygen through the orifice is less than that which will produce over-oxygenation of the patient if delivered on a continuous basis. Thus 9 no matter how fast the patient breathes, there will be an upper limit to the amount of oxygen which will be delivered to the patient per unit of time.
There is also provided another line 92 communicating between the interior of containment means 95 and port 90d of valve 90. The opposite valve port, 90c, is connected to cannula 26 which terminates in nares (or mask) 27. I~ the valve position shown, line 92 is isolated from cannula 26 by valve 90. Sensor 28 may be connected by 35 way of line 29 to cannula 26. Upon detection of tha start of an inhalation, sensor 28 produces a signal which is transmitted to control means 31 by means 30. Control means 31, in turn, causes actuator 93 to cbange the valve to its other position. In this other ,, , ~ , - : , :, . ::, . . . .
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position, li~e 22 is lsolated from source line 23 whiLe line 92 is connected to cannula 26 releasing the dose of gas within containment means 95 and allowing that dose to flow through the cannula for breathing by the patient.
Turning now to Figure 8, there is shown a control circuit which may be used with any or all of the containment means embodiments of this invention. In the circuit shown, sensor 28 is arranged to produce a signal only upon the detection of the onset of an inhalation. That signal 30 is transmitted to a counting and controlling means 115. Means 115 is arranged to count signals produced by sensor 28 and, after receiving a pre-selected number of signals from sensor 28, to transmlt an activating signal 116 to a relay 120 and to a time delay relay 121. Activating signal 116 triggers relay 120 act$vating selenoid coil 123 of flow control valve 15 124 by way of the circuit comprising conductors 125 and 126, power supply 127 and conductors 128 and 129. Flow control valve 124 may be a three-port, two-position valve as in Figure 2 or may be a Eour-port, two-position valve as shown in Figures 4 and 7, or functional e~uivalents thereof. Signal 116 also activates interval timer 121 20 which, upon receiving the si~nal, initiates a timed cycle of power from power supply 127 by way of conductors 129, 130 and 131 causing solenoid coil 132 to change the position of valve 133. Valve 133 is a simple two-way isolating valve which is inserted into line 29 connecting sensor 28 with cannula 26. Valve 133 is arranged to bs in 2~ the closed position whlle solenoid coil 132 is activated by interval timer 121. The power pulse produced by interval timer 121`is long enough, typically about 1/2 second, to shield the sensor 28 from the rush of respirating gas released upon the onset of an inhalation by movement of flow control valve 124. At the end of timed interval, 3 solenoid 132 is de-energized and valve 133 returns to the open position re-connecting sensor 28 with cannula 26.
Incorporation o~ counting and controlling means 115 into the circuit allows greater flexibility in the dispensing of gas doses to a patient. Means 115 may be set so as to produce a signal 116, and 3~ thereby to deliver a prescribed single dose quantity of supplemental oxygen, on each inhalation signal, on every second inhalation signal, on every third inhalation signal, and so forth. In this way maximum flexibility in the dispensing of supplemental oxygen to a patient may , ~ , ; - . ::
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be attained.
In each and all of the embodiments of ,his invention, the cannula, or other gas delivery means to the patient, is never in direct communication with the source o~ the respirating gas. Prior 5 art devices can be generally characterlzed is provlding direct communication, or an open flow path, between the source of the respirating gas and the patient while gas delivery is in progress.
Pre-metering and temporarily storing each unit dose of respirating gas, as the devices of this invention do, inherently provides safety lO features not present in conventional gas delivery systems.
As has been described in relation to the various embodiments, this invention provides both an improved and a simplified way to dispense gases to a patient by effecting a known displacement. The duration of delivery can still be relatively short so as to improve 15 the patient's utilization of the dose but the duration of delivery does not need to be precisely controlled. In fact, by using the method and apparatus of this invention, the time of delivery will tend to be non-linear with variations in prescribed dosages.
Other embodiments of and uses for this invention will be apparent 20 to those skilled in the art without departing from the spirit and scope of the following claims.

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Claims (23)

1. A device for supplying premeasured doses of respirating gas to a patient in synchronization with the respiratory cycle of said patient, comprising:
a source of respirating gas at relatively high pressure;
containment means having a volume sized to measure a prescribed single dose quantity of said respirating gas and to temporarily store said measured dose;
means for sensing the onset of inhalations of said patient and for producing signals in response to said sensing;
first gas flow routing means acting in response to a sensed inhalation signal for releasing said measured dose of respirating gas from said containment means;
cannula means for conveying said released gas from said containment means through said flow routing means to said patient, and second gas flow routing means for refilling said containment means from said respirating gas source.

2. The device of claim 1 wherein said first and second gas flow routing means comprise a three-way valve having a common port and two option ports; the common port communicating with the interior of said containment means, one of said two option ports communicating with said cannula means and the other of said two option ports connected to said respirating gas source.

3. The device of claim 2 wherein said means for sensing the onset of inhalation comprises a sensor which produces a first electrical signal in response to said sensing and wherein said signal is transmitted to a flip-flop relay having a power supply associated therewith; wherein said three-way valve is solenoid operated; and wherein said electrical signal causes said relay and said solenoid to move said valve to that position connecting the interior of said containment means to said cannula means whereupon said single dose quantity of respirating gas is released from said containment means and conveyed to the patient.

4. The device of claim 3 wherein said sensor produces a second electrical signal representative of the onset of an exhalation, said second electrical signal being transmitted to said flip-flop relay causing said relay and said solenoid to move said valve to its other position connecting the interior of said containment means to said respirating gas source whereupon said containment means is refilled from said gas source.

5. The device of claim 3 wherein said sensor is arranged to produce an electrical signal only upon the onset of an inhalation, wherein said containment means is arranged to produce a different electrical signal upon release of said gas dose, and wherein said different electrical signal is transmitted to said relay causing said relay and said solenoid to move said valve to its other position connecting the interior of said containment means to said respirating gas source whereupon said containment means is refilled from said gas source.

6. The device of claim 2 wherein said means for sensing the onset of inhalations comprises a sensor which produces a first electrical signal in response to said sensing and wherein said signal is transmitted to and triggers an interval timer; wherein said three-way valve is solenoid operated, and wherein said interval timer activates the solenoid of said valve causing the valve to move from a first position to a second position, the duration of said interval being sufficient to allow release of said gas dose from said containment means.

7. The device of claim 1 wherein said means for sensing the onset of inhalations comprises a sensor adapted to produce a first signal in response to said sensing and wherein said first and second gas flow routing means comprise a two-position multi-ported valve arranged in one position to connect said source of respirating gas to the interior of said containment means and to connect said sensor with said cannula means, said cannula means communicating with the nasal cavity of said patient, and when said valve is in its other position, isolating said sensor and connecting the interior of said containment means with said cannula means whereupon a single dose quantity of respirating gas is released from said containment means and conveyed to said patient.

8. The device of claim 7 wherein said valve is powered to move from one position to its other position by activating means, said activating means being either a pneumatic activator or an electric solenoid coil.

9. The device of claim 8 wherein said first signal triggers an interval timer which, in turn activates a solenoid coil of said valve for a time interval causing the valve to move to its other position, the duration of said interval being sufficient to allow release of said gas dose from said containment means.

10. The device of claim 8 including means adapted to produce a second signal upon completion of the release of said gas dose from said containment means.

11. The device of claim 10 wherein said first signal triggers a flip-flop relay which activates a solenoid coil associated with said valve causing the valve to move to its other position and wherein said second signal again triggers said relay whereupon said relay, acting upon said solenoid coil, causes said valve to return to its first position.

12. The device of claim 1 wherein said containment means comprises a cylinder having a reciprocating piston disposed therein, the piston urged toward one end of said cylinder by resilient restoring means, and the length of travel of said piston within the cylinder being limited by a stop.

13. The device of claim 12 wherein the position of said stop is adjustable so as to allow varying of the volume displaced by one stroke of said piston within the cylinder.

14. The device of claim 12 wherein said resilient restoring means comprises a mechanical spring.

15. The device of claim 12 wherein said resilient restoring means comprises a pneumatic chamber.

16. The device of claim 12 wherein said piston includes a diaphragm in the shape of a truncated cone with its center fastened to the head of said piston and its outer flange sealingly clamped to said cylinder; said diaphragm alternately rolling and unrolling on the skirt of said piston and the wall of said cylinder as the piston travels back and forth.

17. The device of claim 1 wherein said containment means comprise a container having a volume sized to hold a prescribed dose of respirating gas, said prescribed dose being that quantity of gas delivered to the patient at a single breath.

18. The device of claim 17 wherein said container comprises a cylinder containing a piston, said piston being arranged to be fixedly positioned at multiple locations within said cylinder to thereby deliver different prescribed doses of respirating gas.

- 16 .

19. The device of claim 1 including means to count signals produced in response to sensed inhalations and to activate said first gas flow routing means after a pre-selected number of signals has been counted.

20. A method for administering precisely premeasured doses of respirating gas to a patient in synchronization with the respiratory cycle of said patient comprising the following steps:
filling a containment means with a respirating gas at relatively high pressure, the volume of said containment means adjusted in relation to said gas pressure so that a prescribed single dose quantity of respirating gas is held in said containment means;
sensing the onset of inhalations of said patient and producing signals in response to said sensing;
releasing said dose of respirating gas in response to a sensed inhalation signal and conveying said released gas dose to said patient for breathing, and refilling said containment means with another single dose quantity of respirating gas.

21. The method of claim 20 wherein said prescribed single dose quantity of respirating gas is released to said patient by displacing said single dose of gas from a cylinder by movement of a piston within said cylinder through a fixed distance.

22. The method of claim 20 wherein said prescribed single dose quantity of respirating gas is released to said patient by introducing said gas into a container having a fixed volume and pressurizing said gas to a known pressure higher than atmospheric and thereafter allowing the pressurized gas within said container to blow down to essentially atmospheric pressure through cannula means operably arranged to convey said gas to said patient.

23. The method of claim 21 wherein said piston and cylinder are sized one relative to the other such that the free space within the cylinder with the piston in place therein is proportional to the volume of said premeasured gas dose.